1999
DOI: 10.1006/phrs.1998.0424
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Spotlight on the Continual Applicability of Routine Plasma Monitoring Antiepileptic Drugs in the Treatment of Epilepsy

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Cited by 10 publications
(4 citation statements)
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“…10 Plasma concentrations of drugs are monitored at regular intervals to evaluate therapy efficiency in patients with epilepsy, especially in patients who receive two or more antiepileptic drugs simultaneously. 1,11 According to our study results, it was found that the average plasma carbamazepine (3.39 + 0.27 mg/ml; Figure 1) and valproic acid (44.44 + 2.51 mg/ml; Figure 3) concentrations decreased below the therapeutic index, and the decrease was significant when administered in combination with phenytoin. The average plasma carbamazepine concentration decreased when administered in combination with phenytoin; this observation was similar to that of the other studies.…”
Section: Discussionmentioning
confidence: 73%
See 1 more Smart Citation
“…10 Plasma concentrations of drugs are monitored at regular intervals to evaluate therapy efficiency in patients with epilepsy, especially in patients who receive two or more antiepileptic drugs simultaneously. 1,11 According to our study results, it was found that the average plasma carbamazepine (3.39 + 0.27 mg/ml; Figure 1) and valproic acid (44.44 + 2.51 mg/ml; Figure 3) concentrations decreased below the therapeutic index, and the decrease was significant when administered in combination with phenytoin. The average plasma carbamazepine concentration decreased when administered in combination with phenytoin; this observation was similar to that of the other studies.…”
Section: Discussionmentioning
confidence: 73%
“…10 Plasma concentrations of drugs are monitored at regular intervals to evaluate therapy efficiency in patients with epilepsy, especially in patients who receive two or more antiepileptic drugs simultaneously. 1,11…”
Section: Discussionmentioning
confidence: 99%
“…[1][2][3] Whiting et al 4 proposed that a population pharmacokinetics (PPK) model could be imported to a Bayesian module of Nonlinear Mixed Effects Model (NONMEM) software, which may lead to increased efficiency in dosage adjustment. [1][2][3] Whiting et al 4 proposed that a population pharmacokinetics (PPK) model could be imported to a Bayesian module of Nonlinear Mixed Effects Model (NONMEM) software, which may lead to increased efficiency in dosage adjustment.…”
Section: Introductionmentioning
confidence: 99%
“…These are summarized in Table 3. 12,29,59,62 Ultimately, patients receiving VPA demonstrate widely variable pharmacokinetic parameters due to differences in protein binding and saturation, effects on clearance, and possible diurnal variations. Attempts to define a dose-concentration relationship have found poor albeit statistically significant correlations, and are realistically unlikely to be successful given valproate's fluctuating protein binding characteristics.…”
Section: Vpa Dose-concentration Relationshipmentioning
confidence: 99%